A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982270



Internal ID18617465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62624366..62687316hg38UCSC Ensembl
Innerchr9:46935667..46998617hg19UCSC Ensembl
Innerchr9:46775487..46838437hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg3862951
hg1962951
hg1862951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2544430, nssv2544432, nssv2544428, nssv2544431, nssv2544429, nssv2544433, nssv2544435, nssv2544437, nssv2544436, nssv2544434
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982270
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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